TWI580758B - 新穎照明裝置 - Google Patents

新穎照明裝置 Download PDF

Info

Publication number: TWI580758B
Authority: TW; Taiwan
Prior art keywords: bis; organic fluorescent; color converter; indole; group
Prior art date: 2011-02-24

Application number

TW101106252A

Other languages

English (en)

Chinese (zh)

Other versions

TW201239065A (en

Inventor

傑哈德瓦根布拉斯特

馬汀柯內曼

凱澤赫拉爾杜斯德

索林伊凡諾為奇

麥可派特斯

麥特斯米勒

羅伯特宋德

Original Assignee

巴地斯顏料化工廠

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2011-02-24

Filing date

2012-02-24

Publication date

2017-05-01

2012-02-24 Application filed by 巴地斯顏料化工廠 filed Critical 巴地斯顏料化工廠

2012-10-01 Publication of TW201239065A publication Critical patent/TW201239065A/zh

2017-05-01 Application granted granted Critical

2017-05-01 Publication of TWI580758B publication Critical patent/TWI580758B/zh

Links

238000005286 illumination Methods 0.000 title claims description 12
239000007850 fluorescent dye Substances 0.000 claims description 45
239000003086 colorant Substances 0.000 claims description 38
239000011159 matrix material Substances 0.000 claims description 34
239000004793 Polystyrene Substances 0.000 claims description 32
229920000515 polycarbonate Polymers 0.000 claims description 30
229920002223 polystyrene Polymers 0.000 claims description 30
239000004417 polycarbonate Substances 0.000 claims description 29
229910052757 nitrogen Inorganic materials 0.000 claims description 23
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 21
-1 Isopropylphenoxy Chemical group 0.000 claims description 20
239000000203 mixture Substances 0.000 claims description 16
229910052736 halogen Inorganic materials 0.000 claims description 11
150000001875 compounds Chemical class 0.000 claims description 10
125000001624 naphthyl group Chemical group 0.000 claims description 9
125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
AVMSWPWPYJVYKY-UHFFFAOYSA-N 2-Methylpropyl formate Chemical compound CC(C)COC=O AVMSWPWPYJVYKY-UHFFFAOYSA-N 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
238000006243 chemical reaction Methods 0.000 claims description 6
HTABYAMMLSMTBX-UHFFFAOYSA-N 3-carbamoyl-1-[2,6-di(propan-2-yl)phenyl]indole-4-carboxylic acid Chemical compound C(C)(C)C1=C(C(=CC=C1)C(C)C)N1C=C(C=2C(=CC=CC1=2)C(=O)O)C(O)=N HTABYAMMLSMTBX-UHFFFAOYSA-N 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
OAEQYDZVVPONKW-UHFFFAOYSA-N butan-2-yl formate Chemical compound CCC(C)OC=O OAEQYDZVVPONKW-UHFFFAOYSA-N 0.000 claims description 4
239000002245 particle Substances 0.000 claims description 4
RUPAXCPQAAOIPB-UHFFFAOYSA-N tert-butyl formate Chemical compound CC(C)(C)OC=O RUPAXCPQAAOIPB-UHFFFAOYSA-N 0.000 claims description 4
239000003570 air Substances 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
239000011261 inert gas Substances 0.000 claims description 3
229920006254 polymer film Polymers 0.000 claims description 3
239000002904 solvent Substances 0.000 claims description 3
238000001746 injection moulding Methods 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims 4
125000005577 anthracene group Chemical group 0.000 claims 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
239000012463 white pigment Substances 0.000 claims 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 21
239000010410 layer Substances 0.000 description 20
229920000642 polymer Polymers 0.000 description 14
230000005855 radiation Effects 0.000 description 11
235000012431 wafers Nutrition 0.000 description 11
239000000463 material Substances 0.000 description 10
229920001577 copolymer Polymers 0.000 description 9
239000000975 dye Substances 0.000 description 8
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
150000001454 anthracenes Chemical class 0.000 description 7
150000002367 halogens Chemical class 0.000 description 7
239000000049 pigment Substances 0.000 description 7
239000006185 dispersion Substances 0.000 description 6
229920001519 homopolymer Polymers 0.000 description 5
238000006862 quantum yield reaction Methods 0.000 description 5
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 4
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
NMJJFJNHVMGPGM-UHFFFAOYSA-N butyl formate Chemical compound CCCCOC=O NMJJFJNHVMGPGM-UHFFFAOYSA-N 0.000 description 4
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
108010043121 Green Fluorescent Proteins Proteins 0.000 description 3
238000000295 emission spectrum Methods 0.000 description 3
239000011521 glass Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
239000012860 organic pigment Substances 0.000 description 3
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
150000003440 styrenes Chemical class 0.000 description 3
239000000758 substrate Substances 0.000 description 3
UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 description 2
VEKMJKMSTPFHQD-UHFFFAOYSA-N 1h-benzimidazole-2-carbonitrile Chemical group C1=CC=C2NC(C#N)=NC2=C1 VEKMJKMSTPFHQD-UHFFFAOYSA-N 0.000 description 2
VGKYEIFFSOPYEW-UHFFFAOYSA-N 2-methyl-4-[(4-phenyldiazenylphenyl)diazenyl]phenol Chemical compound Cc1cc(ccc1O)N=Nc1ccc(cc1)N=Nc1ccccc1 VGKYEIFFSOPYEW-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
241000611421 Elia Species 0.000 description 2
229940123457 Free radical scavenger Drugs 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
229910010413 TiO 2 Inorganic materials 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
238000002835 absorbance Methods 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
JNDMLEXHDPKVFC-UHFFFAOYSA-N aluminum;oxygen(2-);yttrium(3+) Chemical compound [O-2].[O-2].[O-2].[Al+3].[Y+3] JNDMLEXHDPKVFC-UHFFFAOYSA-N 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
239000003822 epoxy resin Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
230000005284 excitation Effects 0.000 description 2
229920002521 macromolecule Polymers 0.000 description 2
238000005259 measurement Methods 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
239000000178 monomer Substances 0.000 description 2
150000002790 naphthalenes Chemical class 0.000 description 2
229920000620 organic polymer Polymers 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 2
229920000647 polyepoxide Polymers 0.000 description 2
229920000193 polymethacrylate Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000010526 radical polymerization reaction Methods 0.000 description 2
239000002516 radical scavenger Substances 0.000 description 2
239000004065 semiconductor Substances 0.000 description 2
239000002356 single layer Substances 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
239000004408 titanium dioxide Substances 0.000 description 2
229910019901 yttrium aluminum garnet Inorganic materials 0.000 description 2
XWZOKATWICIEMU-UHFFFAOYSA-N (3,5-difluoro-4-formylphenyl)boronic acid Chemical compound OB(O)C1=CC(F)=C(C=O)C(F)=C1 XWZOKATWICIEMU-UHFFFAOYSA-N 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
FVLTXCPGQRZFBQ-UHFFFAOYSA-N 1-butoxy-4-ethenylbenzene Chemical compound CCCCOC1=CC=C(C=C)C=C1 FVLTXCPGQRZFBQ-UHFFFAOYSA-N 0.000 description 1
NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
GRFNSWBVXHLTCI-UHFFFAOYSA-N 1-ethenyl-4-[(2-methylpropan-2-yl)oxy]benzene Chemical compound CC(C)(C)OC1=CC=C(C=C)C=C1 GRFNSWBVXHLTCI-UHFFFAOYSA-N 0.000 description 1
QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
HTKHARRVPIOLGW-UHFFFAOYSA-N 2-methylpropoxymethanediol Chemical compound CC(C)COC(O)O HTKHARRVPIOLGW-UHFFFAOYSA-N 0.000 description 1
BGQDCDRDPCVLJE-UHFFFAOYSA-N 3-methoxybenzo[b]phenalen-7-one Chemical compound C12=CC=CC=C2C(=O)C2=CC=CC3=C2C1=CC=C3OC BGQDCDRDPCVLJE-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 description 1
ACYXOHNDKRVKLH-UHFFFAOYSA-N 5-phenylpenta-2,4-dienenitrile prop-2-enoic acid Chemical compound OC(=O)C=C.N#CC=CC=CC1=CC=CC=C1 ACYXOHNDKRVKLH-UHFFFAOYSA-N 0.000 description 1
FQLZTPSAVDHUKS-UHFFFAOYSA-N 6-amino-2-(2,4-dimethylphenyl)benzo[de]isoquinoline-1,3-dione Chemical compound CC1=CC(C)=CC=C1N(C1=O)C(=O)C2=C3C1=CC=CC3=C(N)C=C2 FQLZTPSAVDHUKS-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
230000005457 Black-body radiation Effects 0.000 description 1
241000397426 Centroberyx lineatus Species 0.000 description 1
PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
VAYOSLLFUXYJDT-RDTXWAMCSA-N Lysergic acid diethylamide Chemical compound C1=CC(C=2[C@H](N(C)C[C@@H](C=2)C(=O)N(CC)CC)C2)=C3C2=CNC3=C1 VAYOSLLFUXYJDT-RDTXWAMCSA-N 0.000 description 1
239000004425 Makrolon Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
229920005373 Plexiglas® 6N Polymers 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
239000005083 Zinc sulfide Substances 0.000 description 1
UIPKUCOYESFEMJ-UHFFFAOYSA-N [Zn].[La] Chemical compound [Zn].[La] UIPKUCOYESFEMJ-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
238000010539 anionic addition polymerization reaction Methods 0.000 description 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
239000001000 anthraquinone dye Substances 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
238000012662 bulk polymerization Methods 0.000 description 1
BZDKYAZTCWRUDZ-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate;prop-2-enenitrile;styrene Chemical compound C=CC=C.C=CC#N.COC(=O)C(C)=C.C=CC1=CC=CC=C1 BZDKYAZTCWRUDZ-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000010538 cationic polymerization reaction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000001186 cumulative effect Effects 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
230000005611 electricity Effects 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
150000002118 epoxides Chemical class 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
150000002475 indoles Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011147 inorganic material Substances 0.000 description 1
230000010354 integration Effects 0.000 description 1
230000001678 irradiating effect Effects 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
230000031700 light absorption Effects 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
229920012128 methyl methacrylate acrylonitrile butadiene styrene Polymers 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
229920005787 opaque polymer Polymers 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920001083 polybutene Polymers 0.000 description 1
238000012643 polycondensation polymerization Methods 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920002098 polyfluorene Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920005553 polystyrene-acrylate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
238000012545 processing Methods 0.000 description 1
125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
239000001044 red dye Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
238000010557 suspension polymerization reaction Methods 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000012360 testing method Methods 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000001043 yellow dye Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/02—Use of particular materials as binders, particle coatings or suspension media therefor
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21K—NON-ELECTRIC LIGHT SOURCES USING LUMINESCENCE; LIGHT SOURCES USING ELECTROCHEMILUMINESCENCE; LIGHT SOURCES USING CHARGES OF COMBUSTIBLE MATERIAL; LIGHT SOURCES USING SEMICONDUCTOR DEVICES AS LIGHT-GENERATING ELEMENTS; LIGHT SOURCES NOT OTHERWISE PROVIDED FOR
- F21K9/00—Light sources using semiconductor devices as light-generating elements, e.g. using light-emitting diodes [LED] or lasers
- F21K9/60—Optical arrangements integrated in the light source, e.g. for improving the colour rendering index or the light extraction
- F21K9/64—Optical arrangements integrated in the light source, e.g. for improving the colour rendering index or the light extraction using wavelength conversion means distinct or spaced from the light-generating element, e.g. a remote phosphor layer
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V9/00—Elements for modifying spectral properties, polarisation or intensity of the light emitted, e.g. filters
- F21V9/30—Elements containing photoluminescent material distinct from or spaced from the light source
- F21V9/38—Combination of two or more photoluminescent elements of different materials
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/48—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor body packages
- H01L33/50—Wavelength conversion elements
- H01L33/501—Wavelength conversion elements characterised by the materials, e.g. binder
- H01L33/502—Wavelength conversion materials
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/10—Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V9/00—Elements for modifying spectral properties, polarisation or intensity of the light emitted, e.g. filters
- F21V9/30—Elements containing photoluminescent material distinct from or spaced from the light source

Landscapes

Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Materials Engineering (AREA)
Organic Chemistry (AREA)
Physics & Mathematics (AREA)
Microelectronics & Electronic Packaging (AREA)
Manufacturing & Machinery (AREA)
Spectroscopy & Molecular Physics (AREA)
General Engineering & Computer Science (AREA)
Optics & Photonics (AREA)
Computer Hardware Design (AREA)
Power Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Led Device Packages (AREA)
Optical Filters (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Electroluminescent Light Sources (AREA)

TW101106252A 2011-02-24 2012-02-24 新穎照明裝置 TWI580758B (zh)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date
US201161446139P	2011-02-24	2011-02-24
EP11155901		2011-02-24
EP11165344		2011-05-09

Publications (2)

Publication Number	Publication Date
TW201239065A TW201239065A (en)	2012-10-01
TWI580758B true TWI580758B (zh)	2017-05-01

Family

ID=46720121

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW101106252A TWI580758B (zh)	2011-02-24	2012-02-24	新穎照明裝置

Country Status (9)

Country	Link
US (2)	US9236535B2 (fr)
EP (1)	EP2678403B1 (fr)
JP (2)	JP6305063B2 (fr)
KR (1)	KR101970021B1 (fr)
CN (1)	CN103380192B (fr)
PL (1)	PL2678403T3 (fr)
RU (1)	RU2601329C2 (fr)
TW (1)	TWI580758B (fr)
WO (1)	WO2012113884A1 (fr)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP6305063B2 (ja) *	2011-02-24	2018-04-04	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	新規な照明装置
CN103517964B (zh)	2011-05-10	2018-05-18	巴斯夫欧洲公司	新型颜色转换器
US9406848B2 (en)	2011-06-10	2016-08-02	Basf Se	Color converter
CN104919613A (zh)	2013-01-15	2015-09-16	巴斯夫欧洲公司	三角烯低聚物和聚合物及其作为空穴传导材料的用途
CN105189695B (zh) *	2013-02-11	2018-03-13	飞利浦照明控股有限公司	苯氧基取代的二萘嵌苯‑3,4,9,10‑四羧酸二酰亚胺有机红光发射体、及使用其的发光器件
WO2014122071A1 (fr)	2013-02-11	2014-08-14	Koninklijke Philips N.V.	Augmentation de la durée de vie d'un luminophore organique à l'aide d'une excitation différente de l'excitation maximale
US9969932B2 (en)	2013-03-01	2018-05-15	Philips Lighting Holding B.V.	Class of green/yellow emitting phosphors based on benzoxanthene derivatives for LED lighting
US9204598B2 (en)	2013-05-27	2015-12-08	Saudi Basic Indsutries Corporation	Solar energy funneling using thermoplastics for agricultural applications
US9598632B2 (en)	2013-11-21	2017-03-21	Ford Global Technologies, Llc	Method for depositing photoluminescent material
DE102014100837A1 (de) *	2014-01-24	2015-07-30	Osram Opto Semiconductors Gmbh	Lichtemittierendes Bauelement und Verfahren zur Herstellung eines lichtemittierenden Bauelements
WO2015169935A1 (fr) *	2014-05-09	2015-11-12	Basf Se	Composés de pérylène cyanés
TWI617659B (zh) *	2015-01-31	2018-03-11	Lg 化學股份有限公司	色彩轉換膜、其製造方法、背光單元和顯示設備
KR20170129766A (ko)	2015-03-26	2017-11-27	바스프 에스이	시안화 벤조크산텐 및 벤조티오크산텐 화합물
EP3072887B1 (fr)	2015-03-26	2017-10-18	Basf Se	N, n'-bis (2,6-diisopropylphenyl) -1,7-di (2,6-diphenylphenoxy) perylene-3,4; 9,10-tetracarboximide, n, n'-bis (2,6-diisopropylphenyl) -1,6-di (2,6-diphenylphenoxy) perylene-3,4; 9,10-tetracarboximide et son utilisation
CN107924976B (zh) *	2015-08-17	2021-01-08	无限关节内窥镜检查公司	集成光源
WO2017034370A1 (fr) *	2015-08-26	2017-03-02	욱성화학주식회사	Composé à base de pérylène, procédé de préparation associé, et colorant fluorescent le comprenant
WO2017087448A1 (fr)	2015-11-16	2017-05-26	Infinite Arthroscopy Inc, Limited	Système d'imagerie médicale sans fil
JP6949033B2 (ja)	2016-01-14	2021-10-13	ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆＳｅ	剛直な２，２’−ビフェノキシ架橋を有するペリレンビスイミド
CN109328313A (zh)	2016-04-27	2019-02-12	巴斯夫欧洲公司	层压发光器件
KR101983694B1 (ko) *	2016-07-27	2019-05-29	삼성에스디아이 주식회사	신규한 화합물, 이를 포함하는 감광성 수지 조성물 및 컬러필터
TWI770068B (zh)	2016-10-06	2022-07-11	德商巴地斯顏料化工廠	經2-苯基苯氧基取代之苝雙醯亞胺化合物及其用途
WO2018108827A1 (fr)	2016-12-12	2018-06-21	CSEM Centre Suisse d'Electronique et de Microtechnique SA - Recherche et Développement	Dispositif électroluminescent
JP7065883B2 (ja)	2017-01-18	2022-05-12	ビーエーエスエフソシエタス・ヨーロピア	色変換体としての１，６，７，１２－テトラ－（２－イソプロピルフェノキシ）置換ペリレンテトラカルボン酸ジイミド
WO2018141742A1 (fr)	2017-02-03	2018-08-09	Basf Se	Vitrage feuilleté comprenant une structure composite de couches feuilletées
EP4250721A3 (fr)	2017-02-15	2024-02-07	Lazurite Holdings LLC	Système d'imagerie médicale sans fil comprenant une unité de tête et un câble lumineux qui comprend une source lumineuse intégrée
KR20190132659A (ko) *	2017-03-24	2019-11-28	바스프 에스이	색 변환기를 위한 매트릭스 물질로서의 폴리(에틸렌 푸란-2,5-디카르복실레이트)
TWI806892B (zh) *	2017-08-24	2023-07-01	德商巴地斯顏料化工廠	用於傳輸資料及在可見光譜範圍內發射電磁輻射的傳輸器及資料傳輸系統
JP6481987B1 (ja) *	2018-01-24	2019-03-13	ベスパック株式会社	白色ｌｅｄ光源用照明カバー及び製造方法
EP3804669A4 (fr) *	2018-05-29	2022-01-05	Neuroceuticals Inc.	Dispositif d'éclairage intraoculaire
KR102432808B1 (ko) *	2018-08-31	2022-08-16	동우 화인켐 주식회사	백색 수지 조성물, 이를 이용하여 제조된 백 라이트 유닛 및 상기 백 라이트 유닛을 포함하는 표시 장치
USD938584S1 (en)	2020-03-30	2021-12-14	Lazurite Holdings Llc	Hand piece
USD972176S1 (en)	2020-08-06	2022-12-06	Lazurite Holdings Llc	Light source

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TW200641096A (en) *	2005-03-29	2006-12-01	Idemitsu Kosan Co	Red fluorescence conversion medium, color conversion substrate using the same, and light-emitting device
US20100186801A1 (en) *	2007-03-13	2010-07-29	Basf Se	Photovoltaic modules with improved quantum efficiency
CN101908572A (zh) *	2009-06-08	2010-12-08	日东电工株式会社	波长转换片的光学特性控制方法、波长转换片的制造方法、碲化镉系太阳电池用波长转换片及碲化镉系太阳电池

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR100431164B1 (ko) *	1994-11-28	2004-09-16	미네소타 마이닝 앤드 매뉴팩춰링 캄파니	착색내구성및/또는형광내구성이우수한제품
JP3479062B2 (ja)	2001-10-31	2003-12-15	サンユレック株式会社	発光ダイオード
JP4048073B2 (ja) *	2002-03-29	2008-02-13	株式会社ファインラバー研究所	蛍光部材及びこれを用いた発光装置
BR0311626A (pt) *	2002-06-06	2005-06-28	Ilight Technologies Inc	Dispositivo de iluminação para simular luz neon através do uso de cores fluorescentes
DE10244706A1 (de) *	2002-09-24	2004-03-25	Röhm GmbH & Co. KG	Formkörper aus Kunststoff, enthaltend einen Fluoreszenzfarbstoff
JP4636239B2 (ja) *	2003-12-26	2011-02-23	株式会社ファインラバー研究所	Ｌｅｄ用蛍光組成物、ｌｅｄ用蛍光部材及び半導体発光装置
FR2882059B1 (fr) *	2005-02-17	2007-03-23	Arkema Sa	Objet moule presentant un effet multichromatique et dispositif lumineux associe
CN101133684A (zh) *	2005-03-22	2008-02-27	出光兴产株式会社	色变换基板及其制造方法以及发光装置
EP1881741A1 (fr) *	2005-05-12	2008-01-23	Idemitsu Kosan Co., Ltd.	Composition de matériaux de conversion de couleurs et medium de conversion de couleurs la comprenant
DE102005032583A1 (de)	2005-07-11	2007-01-25	Basf Ag	Substituierte Rylenderivate
DE102005054591A1 (de) *	2005-11-14	2007-05-16	Roehm Gmbh	Vorrichtung zur Beleuchtung mit blauen, grünen, gelben oder roten Leuchtdioden
US20100164364A1 (en) *	2006-03-23	2010-07-01	Idemitsu Kosan Co., Ltd.	Light emitting device
DE202006006645U1 (de) *	2006-04-21	2006-07-06	Igus Gmbh	Energieführungskette
DE102007032280A1 (de) *	2007-06-08	2008-12-11	Osram Opto Semiconductors Gmbh	Optoelektronisches Bauelement
US20090078312A1 (en)	2007-09-18	2009-03-26	Basf Se	Verfahren zur herstellung von mit rylentetracarbonsaeurediimiden beschichteten substraten
US7618157B1 (en) *	2008-06-25	2009-11-17	Osram Sylvania Inc.	Tubular blue LED lamp with remote phosphor
DE102008057720A1 (de) *	2008-11-17	2010-05-20	Osram Opto Semiconductors Gmbh	Strahlungsemittierende Vorrichtung
JP5973168B2 (ja) *	2009-02-11	2016-08-23	ナンヤンテクノロジカルユニヴァーシティＮａｎｙａｎｇＴｅｃｈｎｏｌｏｇｉｃａｌＵｎｉｖｅｒｓｉｔｙ	多層外科的プロテーゼ
JP5903039B2 (ja) *	2009-03-19	2016-04-13	コーニンクレッカフィリップスエヌヴェＫｏｎｉｎｋｌｉｊｋｅＰｈｉｌｉｐｓＮ．Ｖ．	色調節装置
EP2412038B1 (fr) *	2009-03-19	2019-01-02	Philips Lighting Holding B.V.	Dispositif d'éclairage avec matériau luminescent à distance
US20120068123A1 (en)	2009-05-26	2012-03-22	Basf Se	Use of phthalocyanine compounds with aryl or hetaryl substituents in organic solar cells
US8724054B2 (en) *	2009-05-27	2014-05-13	Gary Wayne Jones	High efficiency and long life optical spectrum conversion device and process
WO2010145991A1 (fr)	2009-06-18	2010-12-23	Basf Se	Composés de phénanthroazole comme matières de transport de trous pour des dispositifs électroluminescents
US20130109858A1 (en) *	2009-08-20	2013-05-02	Nitto Denko Corporation	Method of synthesizing core-expanded perylene diimide dye and novel core-expanded perylene diimide dye
CN102666560B (zh)	2009-10-14	2015-11-25	巴斯夫欧洲公司	双核铂-卡宾配合物及其在oled中的用途
KR101837095B1 (ko)	2009-10-28	2018-03-09	바스프 에스이	이종 리간드 카르벤 착체 및 유기 전자장치에서의 이의 용도
JP5882223B2 (ja)	2009-12-14	2016-03-09	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	ジアザベンゾイミダゾールカルベン配位子を含む金属錯体及び該錯体をｏｌｅｄにおいて用いる使用
WO2011082961A2 (fr)	2009-12-14	2011-07-14	Basf Se	Procédé de fabrication de surfaces métallisées, surface métallisée et son utilisation
US8895651B2 (en)	2010-02-16	2014-11-25	Basf Se	Composition for printing a seed layer and process for producing conductor tracks
US20110203649A1 (en)	2010-02-19	2011-08-25	Basf Se	Use of indanthrene compounds in organic photovoltaics
US8637857B2 (en)	2010-04-06	2014-01-28	Basf Se	Substituted carbazole derivatives and use thereof in organic electronics
US8691401B2 (en)	2010-04-16	2014-04-08	Basf Se	Bridged benzimidazole-carbene complexes and use thereof in OLEDS
US9359675B2 (en)	2010-04-22	2016-06-07	Basf Se	Producing two-dimensional sandwich nanomaterials based on graphene
JP6057891B2 (ja)	2010-05-03	2017-01-11	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	低温適用のためのカラーフィルター
TWI562898B (en)	2010-05-14	2016-12-21	Basf Se	Process for encapsulating metals and metal oxides with graphene and the use of these materials
KR20130121001A (ko)	2010-05-28	2013-11-05	바스프 에스이	리튬/황 배터리에서 팽창 흑연의 용도
CN102918117B (zh)	2010-06-14	2015-08-12	巴斯夫欧洲公司	黑色二色性染料
US20110308592A1 (en)	2010-06-18	2011-12-22	Basf Se	Use of substituted perylenes in organic solar cells
US20110309344A1 (en)	2010-06-18	2011-12-22	Basf Se	Organic electronic devices comprising a layer of a pyridine compound and a 8-hydroxypquinolinolato earth alkaline metal, or alkali metal complex
US9142792B2 (en)	2010-06-18	2015-09-22	Basf Se	Organic electronic devices comprising a layer comprising at least one metal organic compound and at least one metal oxide
US9203037B2 (en)	2010-06-18	2015-12-01	Basf Se	Organic electronic devices comprising a layer of a dibenzofurane compound and a 8-hydroxypquinolinolato earth alkaline metal, or alkali metal complex
US9067919B2 (en)	2010-07-08	2015-06-30	Basf Se	Use of dibenzofurans and dibenzothiophenes substituted by nitrogen-bonded five-membered heterocyclic rings in organic electronics
CN103154186B (zh)	2010-09-28	2015-07-01	皇家飞利浦电子股份有限公司	具有有机磷光体的发光装置
US9079872B2 (en)	2010-10-07	2015-07-14	Basf Se	Phenanthro[9, 10-B]furans for electronic applications
EP2487218A1 (fr)	2011-02-09	2012-08-15	Koninklijke Philips Electronics N.V.	Matrice polymère avec phosphore organique et sa fabrication
JP6305063B2 (ja) *	2011-02-24	2018-04-04	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	新規な照明装置

2012
- 2012-02-23 JP JP2013554902A patent/JP6305063B2/ja active Active
- 2012-02-23 PL PL12705674T patent/PL2678403T3/pl unknown
- 2012-02-23 WO PCT/EP2012/053102 patent/WO2012113884A1/fr active Application Filing
- 2012-02-23 EP EP12705674.5A patent/EP2678403B1/fr active Active
- 2012-02-23 RU RU2013143030/05A patent/RU2601329C2/ru active IP Right Revival
- 2012-02-23 US US14/001,443 patent/US9236535B2/en active Active
- 2012-02-23 KR KR1020137024435A patent/KR101970021B1/ko active IP Right Grant
- 2012-02-23 CN CN201280009446.XA patent/CN103380192B/zh active Active
- 2012-02-24 TW TW101106252A patent/TWI580758B/zh active
2015
- 2015-12-09 US US14/963,713 patent/US20160084477A1/en not_active Abandoned
2016
- 2016-12-26 JP JP2016250955A patent/JP6521937B2/ja active Active

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TW200641096A (en) *	2005-03-29	2006-12-01	Idemitsu Kosan Co	Red fluorescence conversion medium, color conversion substrate using the same, and light-emitting device
US20100186801A1 (en) *	2007-03-13	2010-07-29	Basf Se	Photovoltaic modules with improved quantum efficiency
CN101908572A (zh) *	2009-06-08	2010-12-08	日东电工株式会社	波长转换片的光学特性控制方法、波长转换片的制造方法、碲化镉系太阳电池用波长转换片及碲化镉系太阳电池

Also Published As

Publication number	Publication date
JP2017058701A (ja)	2017-03-23
JP6521937B2 (ja)	2019-05-29
WO2012113884A1 (fr)	2012-08-30
KR20140009361A (ko)	2014-01-22
US20130334546A1 (en)	2013-12-19
KR101970021B1 (ko)	2019-04-17
JP2014514684A (ja)	2014-06-19
RU2013143030A (ru)	2015-04-10
EP2678403B1 (fr)	2016-02-17
RU2601329C2 (ru)	2016-11-10
JP6305063B2 (ja)	2018-04-04
TW201239065A (en)	2012-10-01
US9236535B2 (en)	2016-01-12
PL2678403T3 (pl)	2016-08-31
CN103380192A (zh)	2013-10-30
CN103380192B (zh)	2016-04-20
EP2678403A1 (fr)	2014-01-01
US20160084477A1 (en)	2016-03-24

Publication	Publication Date	Title
TWI580758B (zh)	2017-05-01	新穎照明裝置
TWI601315B (zh)	2017-10-01	新穎色彩轉換器
TWI670331B (zh)	2019-09-01	氰化之苝化合物
JP7065882B2 (ja)	2022-05-12	シアノアリール置換ナフトイレンベンゾイミダゾール化合物をベースとする蛍光着色剤
US9982189B2 (en)	2018-05-29	Wavelength conversion member and light-emitting device
US20150357528A1 (en)	2015-12-10	Light emitting device
JP2021527155A (ja)	2021-10-11	パラフェニレンビニレンを含む光データ通信システム及び特定のパラフェニレンビニレン
KR102068387B1 (ko)	2020-01-20	함질소 고리 화합물 및 이를 포함하는 색변환 필름
US12031861B2 (en)	2024-07-09	Light conversion device with high uniformity
TW201300704A (zh)	2013-01-01	發光轉換器、磷光體強化光源或具有大於８０之演色性指數之照明器具